Oxycodone Hydrochloride (oxycodone) NDC 71335-0981

Product information

Brand name (proprietary)

Oxycodone Hydrochloride

Generic name (nonproprietary)

oxycodone

Active ingredients

Oxycodone hydrochloride — 5 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203638

Marketing start

Oct 30, 2012

Listing expires

Dec 31, 2026

DEA schedule

CII

Other FDA classes

Full Opioid Agonists (Mechanism)

Identifiers

Product ID 71335-0981_dca003cc-0feb-46b3-aedc-73c20fc7f798SPL ID dca003cc-0feb-46b3-aedc-73c20fc7f798SPL set ID 4e9e945d-5ffc-48de-99fa-3fb36c5bc2b9RxCUI 1049621UNII C1ENJ2TE6C

Pharmacologic class

Opioid Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335098100 followed by a unit qualifier and the quantity Copy

Package 71335-0981-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 203638

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.